Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:108620388-108620647 | Common:6; Rare:131 | ||||
chr4:109815485-109815553 | Rare:22 | ||||
chr4:112231604-112231831 | Common:2; Rare:68 | ||||
chr4:112285761-112285953 | Rare:59 | ||||
chr4:112636885-112637181 | Rare:81 | ||||
chr4:112637394-112637570 | Common:3; Rare:47 | ||||
chr4:119212355-119212767 | Common:5; Rare:131 | ||||
chr4:119300536-119300935 | Common:2; Rare:173 | ||||
chr4:122152225-122152458 | Common:2; Rare:95 | ||||
chr4:122732472-122732708 | Common:1; Rare:69; Clinvar (benign):1 | ||||
chr4:122922963-122923123 | Common:2; Rare:47 | ||||
chr4:127880764-127880934 | Rare:61 | ||||
chr4:128287789-128288048 | Common:3; Rare:99 | ||||
chr4:128288114-128288249 | Common:3; Rare:42 | ||||
chr4:129093494-129093723 | Rare:70 |